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FDA Keeps Class II Recall Active on Bunge Butter Blend Over Unlisted Milk Allergen

Bunge North America is reviewing its allergen labelling processes as the FDA’s Class II warning stays in effect for the 64,800-pound recall.

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Butter

Overview

  • The FDA upgraded the July 14 voluntary recall of NH European Style Butter Blend to a Class II risk category on July 30, indicating potential temporary or medically reversible adverse health consequences.
  • The recall covers 64,800 pounds of butter blend sold in 1-pound blocks under UPC 1 00 78684 73961 2 and lot code 5064036503, distributed to 12 U.S. centres and one in the Dominican Republic.
  • No illnesses or injuries have been reported so far in connection with the undeclared milk allergen in the recalled product.
  • Consumers who purchased the affected lot are urged to stop using the butter, return or discard it, and seek medical attention if they experience allergy symptoms.
  • The incident highlights ongoing food-labelling vulnerabilities and follows similar allergen-declaration errors, prompting calls for stricter quality-control measures.